6338-85-8 Usage
Explanation
The compound consists of 18 carbon atoms, 16 hydrogen atoms, 4 oxygen atoms, and 1 sulfur atom.
Explanation
The compound forms yellow, crystal-like structures when in its solid state.
Explanation
It is widely used in chemical reactions to synthesize other organic compounds and facilitate specific transformations.
Explanation
The compound can participate in a range of chemical reactions, making it valuable in organic synthesis and research.
Explanation
Studies have shown that 1-phenyl-4-(phenylsulfonyl)butane-1,3-dione may have therapeutic effects, such as reducing inflammation and inhibiting the growth of microorganisms.
Explanation
Due to its potential hazards and reactivity, it is essential to follow safety guidelines and use appropriate personal protective equipment when working with 1-phenyl-4-(phenylsulfonyl)butane-1,3-dione.
Physical appearance
Yellow crystalline solid
Common uses
Chemical reagent and intermediate in organic synthesis
Chemical properties
Versatile in various reactions, such as carbon-carbon bond formation and complex organic compound synthesis
Pharmacological properties
Potential anti-inflammatory and antimicrobial effects
Safety precautions
Handle with caution and follow proper safety protocols in laboratory settings
Check Digit Verification of cas no
The CAS Registry Mumber 6338-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6338-85:
(6*6)+(5*3)+(4*3)+(3*8)+(2*8)+(1*5)=108
108 % 10 = 8
So 6338-85-8 is a valid CAS Registry Number.
6338-85-8Relevant academic research and scientific papers
Ru-Catalyzed Chemo- and Enantioselective Hydrogenation of β-Diketones Assisted by the Neighboring Heteroatoms
Li, Wanfang,Lu, Bin,Xie, Xiaomin,Zhang, Zhaoguo
supporting information, p. 5509 - 5513 (2019/08/01)
A highly chemo- and enantioselective hydrogenation of β-diketones was achieved by using [Ru(benzene)(S)-SunPhosCl]Cl for consistency in THF. The neighboring heteroatoms played important roles in guaranteeing the reactivity and controlling the chemoselectivity. These results suggested a potential approach for the clean and facile synthesis of functionalized chiral β-hydroxy ketones, which could otherwise be prepared through much less step-economic transformations.
New access to 1,3-diketones from aldehydes
Fargeas, Valérie,Baalouch, Myriam,Metay, Estelle,Baffreau, Jer?me,Ménard, Delphine,Gosselin, Pascal,Bergé, Jean-Pascal,Barthomeuf, Chantal,Lebreton, Jacques
, p. 10359 - 10364 (2007/10/03)
A simple and efficient methodology to introduce an 1,3-diketone motif from various aldehyde precursors in three steps with good overall yields is described using β-ketosulphone 7 as masked equivalent of acetone. A three-step sequence was studied leading i
